CAS 20300-10-1
:1-Naphthalenecarbothioamide
Description:
1-Naphthalenecarbothioamide, with the CAS number 20300-10-1, is an organic compound characterized by the presence of a naphthalene ring system attached to a carbothioamide functional group. This compound typically exhibits a solid state at room temperature and is known for its aromatic properties due to the naphthalene moiety, which contributes to its stability and potential reactivity. The presence of the thiocarbonyl group (-C(=S)NH2) imparts unique chemical behavior, making it a candidate for various chemical reactions, including nucleophilic substitutions and condensation reactions. It may also exhibit biological activity, which can be of interest in medicinal chemistry. The compound is generally soluble in organic solvents, and its physical properties, such as melting point and boiling point, can vary based on purity and environmental conditions. Safety data should be consulted for handling, as with any chemical substance, to ensure proper precautions are taken due to potential toxicity or reactivity.
Formula:C11H9NS
InChI:InChI=1S/C11H9NS/c12-11(13)10-7-3-5-8-4-1-2-6-9(8)10/h1-7H,(H2,12,13)
InChI key:InChIKey=DRCKUACWKCMOCB-UHFFFAOYSA-N
SMILES:C(N)(=S)C=1C2=C(C=CC1)C=CC=C2
Synonyms:- 1-Naphthalenecarbothioamide
- 1-Naphthalenethiocarboxamide
- 1-Naphthamide, thio-
- 1-Thionaphthamide
- 1-Thionaphthylamide
- NSC 240970
- Naphthalene-1-carbothioamide
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Found 4 products.
Naphthalene-1-carbothioamide
CAS:Formula:C11H9NSPurity:95%Color and Shape:SolidMolecular weight:187.2609Naphthalene-1-Thiocarboxamide
CAS:Naphthalene-1-ThiocarboxamidePurity:97%Molecular weight:187.26g/molNaphthalene-1-thiocarboxamide
CAS:Formula:C11H9NSColor and Shape:No data available.Molecular weight:187.26Naphthalene-1-thiocarboxamide
CAS:<p>Naphthalene-1-thiocarboxamide is a chemical compound with the molecular formula C8H6N2O2S and molecular weight of 228.09 g/mol. It is an organic thiocarboxamide derivative that can be synthesized by reacting naphthalene-1-carboxylic acid with thiourea in the presence of an oxidant and ultrasonic irradiation. This compound has been shown to yield high yields of dimers, which are terminal oxidants, when exposed to light or heat. Naphthalene-1-thiocarboxamide undergoes oxidative dimerization in a reaction time of approximately 3 hours at room temperature in chloranil and oxygen, producing hydroxyl radicals as byproducts. Naphthalene-1-thiocarboxamide has also been used as a catalyst for the sonochemical oxidation process due to its high reactivity and stability.</p>Formula:C11H9NSPurity:Min. 95%Molecular weight:187.26 g/mol



